Quality Analyst - On-site

Description

Job Summary: Quality Analyst to ensure proper execution of the Master Validation Plan, document management, and support for continuous improvement in a regulated sector. Key Responsibilities: 1. Ensure execution of the Master Validation Plan 2. Document management and participation in change control 3. Support for continuous improvement initiatives in a regulated environment A prominent company in the sector requires a Quality Analyst for its team. Main Responsibilities: Ensure proper execution of the Master Validation Plan by participating in activities such as: Equipment and facility qualification Critical system validation Manufacturing and cleaning process validation Annual Product Review Additionally, the role includes: Document management Execution of protocols and reports Participation in change control Non-conformance investigations Supplier evaluation Support for continuous improvement initiatives All of the above performed in strict compliance with applicable regulations. Job Requirements Education: Bachelor's degree in Chemistry, Pharmaceutical Chemistry, Industrial Engineering, or related fields. Additional training (desirable): Knowledge of BPM Validation and quality management systems Additional quality-related training (desirable) Experience: Minimum 1.5 years of experience in quality, production, or validation roles within regulated industries (cosmetics, pharmaceuticals, and/or food). Work Modality: On-site Fully on-site. Monday to Thursday, 7:30 AM–5:00 PM. Friday, 7:30 AM–1:30 PM at the TOCANCIPA plant. Salary: $3,000,000–$3,800,000 + statutory benefits Interested candidates: Apply through this channel. -Requirements- Minimum education: University / Bachelor's degree 2 years of experience Age: between 25 and 37 years Keywords: analyst, quality, qa